To be able to rationalise the observed ABL kinase inhibitory outcomes from the 3D structural point of view, the direct compounds I and II, and also the newly built derivatives 4a, 4b, and five have been docked during the catalytic kinase domains of BCR-ABLWT (PDB code: 3OXZ) and BCR-ABLT315I (PDB https://paxtonsmcsh.blogrelation.com/37171735/the-basic-principles-of-indazole-nmr